Linked Data
dbSNP Id:
rs1878570036
gnomAD v3:
12-68746518-C-T
gnomAD v4:
12-68746518-C-T
MyVariant Identifiers:
chr12:g.69140298C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.68746518C>T , CM000674.2:g.68746518C>T | GRCh38 |
| NC_000012.11:g.69140298C>T , CM000674.1:g.69140298C>T | GRCh37 |
| NC_000012.10:g.67426565C>T | NCBI36 |
| NG_046600.2:g.64568C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319429.7:n.384C>T | ||
| ENST00000398004.4:c.141C>T MANE Select | ENSP00000381089.2:p.Thr47= | |
| ENST00000673712.1:c.141C>T | ENSP00000501065.1:p.Thr47= | |
| ENST00000674096.1:c.141C>T | ENSP00000501130.1:p.Thr47= | |
| ENST00000398004.3:c.141C>T | ENSP00000381089.2:p.Thr47= | |
| NM_018656.2:c.141C>T | NP_061126.2:p.Thr47= | |
| XM_005269006.2:c.141C>T | XP_005269063.1:p.Thr47= | |
| NM_001354997.1:c.141C>T | NP_001341926.1:p.Thr47= | |
| NM_001354998.1:c.141C>T | NP_001341927.1:p.Thr47= | |
| NM_018656.3:c.141C>T | NP_061126.2:p.Thr47= | |
| NR_149143.1:n.433C>T | ||
| NR_149144.1:n.433C>T | ||
| NM_001354997.3:c.141C>T | NP_001341926.1:p.Thr47= | |
| NM_001354998.2:c.141C>T | NP_001341927.1:p.Thr47= | |
| NM_018656.5:c.141C>T MANE Select | NP_061126.2:p.Thr47= | |
| NR_149143.3:n.343C>T | ||
| NR_149144.3:n.343C>T |